Results 121 to 130 of about 665 (159)
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Acrocephalosyndactyly - The Coalesced Hand
European Journal of Pediatric Surgery, 2002Described nearly a century ago, Apert's Syndrome (A.S.) is a rare disorder affecting 1/80,000 children, the mode of inheritance is autosomal dominant or sporadic. Apart from the more obvious skull malformations, extensive and complex hand deformities create several problems for the child's interaction with its environment, preventing normal ...
N, Rebelo +3 more
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Acrocephalosyndactyly (Apert’s syndrome)
The Indian Journal of Pediatrics, 1968A case of Apert’s syndrome in a male child of fourteen years is described and the literature briefly reviewed.
S, Saxena, J, Sharma, O, Saxena
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Acrocephalosyndactyly with report of a case
The British Journal of Radiology, 1953A case of Acrocephalosyndactyly, as first described by Apert, is reported. Reference is made to the high degree of function developed by the patient in grossly deformed hands and feet. There is no evidence that this case is familial and a review and discussion of some of the literature indicates that the condition belongs to the group of skull ...
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Acrocephalosyndactyly, or apert's syndrome
British Journal of Plastic Surgery, 1968Summary 1.Four typical examples of Apert's syndrome are presented. 2.The literature on this subject is reviewed. 3.Current views regarding the aetiology and treatment are discussed. 4.Chromosome studies on one case are reported.
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Acta Paediatrica, 1953
SummaryA case of acrocephalosyndactyly is described. The parents and sibs have been examined by the writers. A pedigree is given and the clinical and genetical features of this rare malformation briefly reviewed.
J A, BOOK, L, HESSELVIK
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SummaryA case of acrocephalosyndactyly is described. The parents and sibs have been examined by the writers. A pedigree is given and the clinical and genetical features of this rare malformation briefly reviewed.
J A, BOOK, L, HESSELVIK
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Acrocephalosyndactyly a Case with Congenital Cardiac Abnormalities
The British Journal of Radiology, 1952Multiple skeletal deformities, syndactyly, polydactyly, and acrocephaly. Angiocardiogram performed at age of 6 weeks. Anomalous double superior venae cavae, pulmonary stenosis, and large interventricular septal defect.
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The foot and Apert's syndrome: acrocephalosyndactyly
Journal of the American Podiatric Medical Association, 1978M, Feinstein, L, Rubin
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